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Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Chronic myeloid leukemia
1 OMIM reference -
3 associated genes
No signs/symptoms info
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Chronic myeloid leukemia

MUC1
(UniProt - OMIM)
 ABL1
(UniProt - OMIM)
UMOD
(UniProt - OMIM)
 BCR
(UniProt - OMIM)
RUNX1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MUC1
(0.79)
ABL1


Citations in the biomedical literature:


Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD
Chronic myeloid leukemia
ABL1 BCR RUNX1



Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
Chronic myeloid leukemia

Synonym(s):
- Autosomal dominant nephronophthisis
Synonym(s):
- Chronic granulocytic leukemia
- Chronic myelogenous leukemia
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.